Canonical Allele Identifier: CA393935244

Gene: LINS1

Linked Data

• gnomAD v4: 15-100573658-T-G
• MyVariant Identifiers: chr15:g.101113863T>G (hg19) ; chr15:g.100573658T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573658T>G , CM000677.2:g.100573658T>G	GRCh38
NC_000015.9:g.101113863T>G , CM000677.1:g.101113863T>G	GRCh37
NC_000015.8:g.98931386T>G	NCBI36
NG_034076.1:g.33583A>C
NG_034076.2:g.34375A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1215A>C MANE Select	ENSP00000318423.8:p.Glu405Asp
ENST00000314742.12:c.1215A>C	ENSP00000318423.8:p.Glu405Asp
ENST00000559149.5:n.1372A>C
ENST00000560133.5:c.858A>C	ENSP00000454929.1:p.Glu286Asp
ENST00000560783.1:c.184A>C
ENST00000561308.5:c.1215A>C	ENSP00000454200.1:p.Glu405Asp
NM_001040616.2:c.1215A>C	NP_001035706.1:p.Glu405Asp
XM_005254941.1:c.1215A>C	XP_005254998.1:p.Glu405Asp
XM_005254943.1:c.1215A>C	XP_005255000.1:p.Glu405Asp
XR_243210.2:n.1318A>C
XR_429464.2:n.1318A>C
XR_931862.1:n.1318A>C
XR_931863.1:n.1318A>C
XR_931864.1:n.1318A>C
NM_001352507.1:c.468A>C	NP_001339436.1:p.Glu156Asp
NM_001352508.1:c.1170A>C	NP_001339437.1:p.Glu390Asp
NR_148017.1:n.1438A>C
NR_148018.1:n.1438A>C
NR_148019.1:n.1442A>C
XM_005254941.2:c.1215A>C	XP_005254998.1:p.Glu405Asp
XM_005254943.2:c.1215A>C	XP_005255000.1:p.Glu405Asp
XM_017022399.2:c.468A>C	XP_016877888.1:p.Glu156Asp
XM_017022400.2:c.468A>C	XP_016877889.1:p.Glu156Asp
XM_024449979.1:c.1215A>C	XP_024305747.1:p.Glu405Asp
XM_024449980.1:c.1215A>C	XP_024305748.1:p.Glu405Asp
XR_001751346.2:n.2230A>C
XR_001751347.2:n.2230A>C
XR_001751348.2:n.2230A>C
XR_002957655.1:n.2230A>C
XR_931862.3:n.2230A>C
NM_001040616.3:c.1215A>C MANE Select	NP_001035706.2:p.Glu405Asp
NM_001352507.2:c.468A>C	NP_001339436.1:p.Glu156Asp
NM_001352508.2:c.1170A>C	NP_001339437.1:p.Glu390Asp
NR_148017.2:n.1382A>C
NR_148018.2:n.1382A>C
NR_148019.2:n.1386A>C